Allele Registry

Canonical Allele Identifier: PA2828750267

Gene: UMOD HGNC NCBI

ClinVar Allele:

75598

ClinVar RCV:

RCV002251329

ClinVar Variation:

64644

HGVS (amino-acid)	Matching Registered Transcripts
NP_001365164.1:p.Cys248Ser	CA264233 NM_001378235.1:c.743G>C CA394984812 NM_001378235.1:c.742T>A